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Chemical Structure| 947179-42-2 Chemical Structure| 947179-42-2

Structure of 947179-42-2

Chemical Structure| 947179-42-2

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Product Details of [ 947179-42-2 ]

CAS No. :947179-42-2
Formula : C9H13BrN2O2S
M.W : 293.18
SMILES Code : O=C(OC(C)(C)C)NC1=NC(C)=C(Br)S1
MDL No. :MFCD12911561

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Application In Synthesis of [ 947179-42-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 947179-42-2 ]

[ 947179-42-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3034-57-9 ]
  • [ 24424-99-5 ]
  • [ 947179-42-2 ]
YieldReaction ConditionsOperation in experiment
64% dmap; In dichloromethane; at 20.0℃; for 20.0h; Step 1: (5-Bromo-4-methyl-thiazol-2-yl)-carbamic acid tert-butyl ester To a solution of 6.46 g (33 mmol) of <strong>[3034-57-9]5-bromo-4-methyl-thiazol-2-ylamine</strong> (CAS [3034-57-9], Kaye and al., J. C. S. Perkin I, 2338 (1981) in 80 ml of dry dichloromethane were added 8.03 g (37 mmol) of di-tert-butyldicarbonate and 0.21 g (2.1 mmol) of 4-dimethylamino-pyridine (DMAP). The reaction was stirred for 20 h at room temperature. After standard workup and purification by flash chromatography (ethyl acetate/heptane 1:2), one obtains the title compound (6.45 g, 64percent) as a light brown solid, MS (ISP): m/e=236.9, 238.9 (M+H)+.
With triethylamine; In dichloromethane; at 20.0℃; A mixture of 50-1 (17.4 g, 90 mmol), Boc2O (25.7 g, 118 mmol) and Et3N (27.3 g, 270mmol) in 200 mL of DCM was stirred at room temperature overnight. The mixture was washedwith water and brine, dried with Na2SO4, filtered and concentrated to give 50-2 (23.2 g, 88percent) asa light yellow crystal.
  • 2
  • [ 3034-57-9 ]
  • Boc2O [ No CAS ]
  • [ 947179-42-2 ]
YieldReaction ConditionsOperation in experiment
88% With triethylamine; In dichloromethane; at 20.0℃; [0182] A mixture ofQj, (17.4 g, 90 mmol), Boc2O (25.7 g, 118 mmol) and Et3N (27.3 g, 270 mmol) in 200 mL of DCM was stirred at room temperature overnight. The mixture was washedwith water and brine, dried with Na2SO4, filtered and concentrated to give 50-2 (23.2 g, 88percent) as a light yellow crystal.
 

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